Ashida T, Kawano Y, Yoshimi H, Akabane S, Kuramochi M, Omae T
Department of Medicine, National Cardiovascular Center Hospital, Osaka, Japan.
J Cardiovasc Pharmacol. 1991;17 Suppl 7:S174-6. doi: 10.1097/00005344-199100177-00049.
We studied the effects of ouabain and verapamil on endothelin-1(ET-1)-induced contraction of the mesenteric artery in prehypertensive spontaneously hypertensive rats (SHRs) and age-matched Wistar-Kyoto (WKY) rats. Rings of mesenteric artery of SHRs and WKY rats aged 4 weeks were superfused with physiological saline solution and isometric tension was measured. ET-1 (10(-9) or 10(-8) M)-induced contractions were significantly larger in WKY rats than in SHRs. ET-1 (10(-7) M)-induced contractions were not significantly different between SHRs and WKY rats. Verapamil markedly inhibited ET-1 (10(-7) M)-induced contractions both in SHRs and in WKY rats. Although the percent inhibition tended to be larger in SHRs than in WKY rats, the difference was not significant. Ouabain significantly increased ET-1 (10(-7) M)-induced contraction in the presence of verapamil both in SHRs and in WKY rats. The increase was significantly greater in SHRs than in WKY rats. As a result, ET-1 (10(-7) M)-induced contractions were significantly greater in SHRs than in WKY rats in the presence of verapamil and ouabain. These results suggest that in ET-1-induced arterial contraction, [Na+]i-mediated [Ca2+]i regulation such as the Na+/Ca2+ exchange system might be greater in SHRs than in WKY rats, and that this might be, at least in part, involved in the pathogenesis or maintenance of hypertension in SHRs.
我们研究了哇巴因和维拉帕米对高血压前期自发性高血压大鼠(SHRs)和年龄匹配的Wistar-Kyoto(WKY)大鼠肠系膜动脉内皮素-1(ET-1)诱导收缩的影响。将4周龄的SHRs和WKY大鼠的肠系膜动脉环用生理盐溶液进行灌流,并测量等长张力。ET-1(10⁻⁹或10⁻⁸M)诱导的收缩在WKY大鼠中比在SHRs中显著更大。ET-1(10⁻⁷M)诱导的收缩在SHRs和WKY大鼠之间无显著差异。维拉帕米显著抑制SHRs和WKY大鼠中ET-1(10⁻⁷M)诱导的收缩。虽然在SHRs中的抑制百分比倾向于比WKY大鼠中的更大,但差异不显著。在维拉帕米存在的情况下,哇巴因显著增加SHRs和WKY大鼠中ET-1(10⁻⁷M)诱导的收缩。在SHRs中的增加比在WKY大鼠中显著更大。结果,在维拉帕米和哇巴因存在的情况下,ET-1(10⁻⁷M)诱导的收缩在SHRs中比在WKY大鼠中显著更大。这些结果表明,在ET-1诱导的动脉收缩中,[Na⁺]i介导的[Ca²⁺]i调节,如Na⁺/Ca²⁺交换系统,在SHRs中可能比在WKY大鼠中更大,并且这可能至少部分参与了SHRs高血压的发病机制或维持。